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dc.contributor.authorWang, ShuQien_US
dc.contributor.authorTasoglu, Savasen_US
dc.contributor.authorChen, Paul Z.en_US
dc.contributor.authorChen, Michaelen_US
dc.contributor.authorAkbas, Ragipen_US
dc.contributor.authorWach, Sonyaen_US
dc.contributor.authorOzdemir, Cenk Ibrahimen_US
dc.contributor.authorGurkan, Umut Atakanen_US
dc.contributor.authorGiguel, Francoise F.en_US
dc.contributor.authorKuritzkes, Daniel R.en_US
dc.contributor.authorDemirci, Utkanen_US
dc.date.accessioned2014-03-11T13:27:11Z
dc.date.issued2014en_US
dc.identifier.citationWang, S., S. Tasoglu, P. Z. Chen, M. Chen, R. Akbas, S. Wach, C. I. Ozdemir, et al. 2014. “Micro-a-fluidics ELISA for Rapid CD4 Cell Count at the Point-of-Care.” Scientific Reports 4 (1): 3796. doi:10.1038/srep03796. http://dx.doi.org/10.1038/srep03796.en
dc.identifier.issn2045-2322en
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:11879637
dc.description.abstractHIV has become one of the most devastating pathogens in human history. Despite fast progress in HIV-related basic research, antiretroviral therapy (ART) remains the most effective method to save AIDS patients' lives. Unfortunately, ART cannot be universally accessed, especially in developing countries, due to the lack of effective treatment monitoring diagnostics. Here, we present an inexpensive, rapid and portable micro-a-fluidic platform, which can streamline the process of an enzyme-linked immunosorbent assay (ELISA) in a fully automated manner for CD4 cell count. The micro-a-fluidic CD4 cell count is achieved by eliminating operational fluid flow via “moving the substrate”, as opposed to “flowing liquid” in traditional ELISA or microfluidic methods. This is the first demonstration of capturing and detecting cells from unprocessed whole blood using the enzyme-linked immunosorbent assay (ELISA) in a microfluidic channel. Combined with cell phone imaging, the presented micro-a-fluidic ELISA platform holds great promise for offering rapid CD4 cell count to scale up much needed ART in resource-constrained settings. The developed system can be extended to multiple areas for ELISA-related assays.en
dc.language.isoen_USen
dc.publisherNature Publishing Groupen
dc.relation.isversionofdoi:10.1038/srep03796en
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898414/pdf/en
dash.licenseLAAen_US
dc.titleMicro-a-fluidics ELISA for Rapid CD4 Cell Count at the Point-of-Careen
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden
dc.relation.journalScientific Reportsen
dash.depositing.authorWang, ShuQien_US
dc.date.available2014-03-11T13:27:11Z
dc.identifier.doi10.1038/srep03796*
dash.authorsorderedfalse
dash.contributor.affiliatedDemirci, Utkan
dash.contributor.affiliatedWang, ShuQi
dash.contributor.affiliatedTasoglu, Savas
dash.contributor.affiliatedChen, Paul
dash.contributor.affiliatedKuritzkes, Daniel


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